U. Schumacher et al., LECTIN HISTOCHEMISTRY OF HUMAN LEUKEMIC MAST-CELLS (HMC-1) TRANSPLANTED INTO SEVERE COMBINED IMMUNODEFICIENT (SCID) MICE, Acta histochemica, 100(1), 1998, pp. 1-9
It is difficult to isolate and impossible to propagate human mast cell
s in tissue culture. As an alternative to the use of human differentia
ted mast cells, a human leukaemic mast cell line (HMC-1), which can be
propagated in vitro, has been employed in a number of studies. Carboh
ydrate binding proteins, lectins, have been used to characterise the t
erminal sugar residues of human mast cells in situ. The aim of the pre
sent study is to characterise the lectin binding sites of HMC-1 cells
transplanted into severe combined immunodeficient (scid) mice. Lectins
specific for the complex carbohydrates, neuraminic acid and N-acetylg
lucosamine residues showed generally a strong uniform binding pattern,
whereas mannose and glucose specific yielded lectins a greater hetero
geneity. This glycotope expression pattern has some similarities with
those of human mast cells in situ, and therefore HMC-1 cells grown in
scid mice constitute a valuable model system for the study of carbohyd
rate expression in human mast cells.